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Inicio Endocrinología y Nutrición Nuevos tratamientos en los tumores neuroendocrinos gastroenteropancreáticos
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Vol. 54. Núm. S1.
Tumores neuroendocrinos gastroenteropancreáticos
Páginas 51-57 (enero 2007)
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Vol. 54. Núm. S1.
Tumores neuroendocrinos gastroenteropancreáticos
Páginas 51-57 (enero 2007)
Tumores neuroendocrinos gastroenteropancreáticos
Acceso a texto completo
Nuevos tratamientos en los tumores neuroendocrinos gastroenteropancreáticos
New treatments in gastroenteropancreatic neuroendocrine tumors
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5661
María Ausencia Toméa,
Autor para correspondencia
sontara@usc.es

Correspondencia: Dra. M.A. Tomé Martínez de Retuerto. Castelo, s/n. 15229 Ames. La Coruña. España.
, Ignacio Duránb, Ramón Salazarc, José Ángel Díazd
a Servicio de Endocrinología. Complejo Hospitalario Universitario de Santiago. CHUS. Santiago de Compostela. La Coruña. España
b Servicio de Oncología Médica. Princess Margaret Hospital. Toronto. Canadá
c Servicio de Oncología Médica. Institut Català d’Oncologia. Barcelona. España.
d Servicio de Endocrinología. Hospital Clínico San Carlos. Madrid. España
Contenido relacionado
Endocrinol Nutr. 2008;55:16410.1016/S1575-0922(08)70666-1
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Bibliografía
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Estadísticas

El tratamiento con análogos de somatostatina radiomarcados es una nueva opción de tratamiento en los pacientes con tumores neuroendocrinos gastroenteropancreáticos inoperables o con enfermedad metastásica. El acoplamiento de distintos isótopos a los análogos de somatostatina permite la unión del complejo a los receptores de somatostatina presentes en la superficie celular de muchos de estos tumores. El tratamiento con radionúclidos persigue la disminución de la masa tumoral con el fin de detener la progresión de le enfermedad, con diversos resultados en función del tipo de isótopo y las dosis utilizadas. Los efectos secundarios de dicho tratamiento incluyen alteraciones hematológicas, hepáticas y renales.

La respuesta de estos tumores al tratamiento con quimioterapia convencional es limitada. El desarrollo de estudios con fármacos antiangiogénicos, inhibidores del receptor del factor de crecimiento epidérmico e inhibidores de mTOR probablemente suponga un gran avance en el tratamiento de los tumores neuroendocrinos.

Palabras clave:
Análogos de somatostatina
Radionúclido
Angiogénesis
Factor de crecimiento epidérmico

Treatment with radiolabeled somatostatin analogs is a novel therapy in patients with inoperable gastroenteropancreatic neuroendocrine tumors or metastatic disease. Coupling of distinct isotopes to somatostatin analogs allows the complexto bind to somatostatin receptors present in the cell surface of many of these tumors. Radionucleotide therapy reduces the tumoral mass with the aim of slowing disease progression and has varying results depending on the type of isotope and the doses used. The secondary effects of this treatment include hematological, hepatic and renal alterations.

The response of these tumors to conventional chemotherapy is limited. The development of studies with antiangiogenic drugs, epidermic growth factor receptor inhibitors, and mTOR inhibitors probably represents a significant advance in the treatment of neuroendocrine tumors.

Key words:
Somatostatin analogs
Radionuclide
Angiogenesis
Epidermal growth factor
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